Somatic mosaicism for copy number variation in differentiated human tissues
Piotrowski, Arkadiusz, Bruder, Carl E.G, Andersson, Robin, de Ståhl, Teresita Diaz, Menzel, Uwe, Sandgren, Johanna, Poplawski, Andrzej, von Tell, Desiree, Crasto, Chiquito, Bogdan, Adam, Bartoszewski, Rafal, Bebok, Zsuzsa, Krzyzanowski, Maciej, Jankowski, Zbigniew, Partridge, E. Christopher, Komorowski, Jan, Dumanski, Jan P
Published in Human mutation (01.09.2008)
Published in Human mutation (01.09.2008)
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Register-based and genetic studies of Prader-Willi syndrome show a high frequency of gonadal tumors and a possible mechanism for tumorigenesis through imprinting relaxation
Maya-González, Carolina, Wessman, Sandra, Lagerstedt-Robinson, Kristina, Taylan, Fulya, Tesi, Bianca, Kuchinskaya, Ekaterina, McCluggage, W Glenn, Poluha, Anna, Holm, Stefan, Nergårdh, Ricard, Díaz De Ståhl, Teresita, Höybye, Charlotte, Tettamanti, Giorgio, Delgado-Vega, Angelica Maria, Skarin Nordenvall, Anna, Nordgren, Ann
Published in Frontiers in medicine (2023)
Published in Frontiers in medicine (2023)
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Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer
Forsberg, Lars A, Rasi, Chiara, Malmqvist, Niklas, Davies, Hanna, Pasupulati, Saichand, Pakalapati, Geeta, Sandgren, Johanna, de Ståhl, Teresita Diaz, Zaghlool, Ammar, Giedraitis, Vilmantas, Lannfelt, Lars, Score, Joannah, Cross, Nicholas C P, Absher, Devin, Janson, Eva Tiensuu, Lindgren, Cecilia M, Morris, Andrew P, Ingelsson, Erik, Lind, Lars, Dumanski, Jan P
Published in Nature genetics (01.06.2014)
Published in Nature genetics (01.06.2014)
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Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles
Bruder, Carl E.G., Piotrowski, Arkadiusz, Gijsbers, Antoinet A.C.J., Andersson, Robin, Erickson, Stephen, Diaz de Ståhl, Teresita, Menzel, Uwe, Sandgren, Johanna, von Tell, Desiree, Poplawski, Andrzej, Crowley, Michael, Crasto, Chiquito, Partridge, E. Christopher, Tiwari, Hemant, Allison, David B., Komorowski, Jan, van Ommen, Gert-Jan B., Boomsma, Dorret I., Pedersen, Nancy L., den Dunnen, Johan T., Wirdefeldt, Karin, Dumanski, Jan P.
Published in American journal of human genetics (01.03.2008)
Published in American journal of human genetics (01.03.2008)
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Journal Article
Somatic mosaicism for chromosome X and Y aneuploidies in monozygotic twins heterozygous for sickle cell disease mutation
Razzaghian, Hamid Reza, Shahi, Mehdi Hayat, Forsberg, Lars A., de Ståhl, Teresita Diaz, Absher, Devin, Dahl, Niklas, Westerman, Maxwell P., Dumanski, Jan P.
Published in American journal of medical genetics. Part A (01.10.2010)
Published in American journal of medical genetics. Part A (01.10.2010)
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Journal Article
Efficient IgG-Mediated Suppression of Primary Antibody Responses in Fcγ Receptor-Deficient Mice
Mikael C. I. Karlsson, Wernersson, Sara, de Stahl, Teresita Diaz, Gustavsson, Susanne, Heyman, Birgitta
Published in Proceedings of the National Academy of Sciences - PNAS (02.03.1999)
Published in Proceedings of the National Academy of Sciences - PNAS (02.03.1999)
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Human cytomegalovirus tegument protein pp65 is detected in all intra- and extra-axial brain tumours independent of the tumour type or grade
Libard, Sylwia, Popova, Svetlana N, Amini, Rose-Marie, Kärjä, Vesa, Pietiläinen, Timo, Hämäläinen, Kirsi M, Sundström, Christer, Hesselager, Göran, Bergqvist, Michael, Ekman, Simon, Zetterling, Maria, Smits, Anja, Nilsson, Pelle, Pfeifer, Susan, de Ståhl, Teresita Diaz, Enblad, Gunilla, Ponten, Fredrik, Alafuzoff, Irina
Published in PloS one (30.09.2014)
Published in PloS one (30.09.2014)
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Journal Article
Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With Cancer
Wadensten, Elisabeth, Wessman, Sandra, Abel, Frida, Diaz De Ståhl, Teresita, Tesi, Bianca, Orsmark Pietras, Christina, Arvidsson, Linda, Taylan, Fulya, Fransson, Susanne, Vogt, Hartmut, Poluha, Anna, Pradhananga, Sailendra, Hellberg, Maria, Lagerstedt-Robinson, Kristina, Raj Somarajan, Praveen, Samuelsson, Sofie, Orrsjö, Sara, Maqbool, Khurram, Henning, Karin, Strid, Tobias, Ek, Torben, Fagman, Henrik, Olsson Bontell, Thomas, Martinsson, Tommy, Puls, Florian, Kogner, Per, Wirta, Valtteri, Pronk, Cornelis Jan, Wille, Joakim, Rosenquist, Richard, Nistér, Monica, Mertens, Fredrik, Sabel, Magnus, Norén-Nyström, Ulrika, Grillner, Pernilla, Nordgren, Ann, Ljungman, Gustaf, Sandgren, Johanna, Gisselsson, David
Published in JCO precision oncology (01.01.2023)
Published in JCO precision oncology (01.01.2023)
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Spatially resolved clonal copy number alterations in benign and malignant tissue
Erickson, Andrew, He, Mengxiao, Berglund, Emelie, Marklund, Maja, Mirzazadeh, Reza, Schultz, Niklas, Kvastad, Linda, Andersson, Alma, Bergenstråhle, Ludvig, Bergenstråhle, Joseph, Larsson, Ludvig, Alonso Galicia, Leire, Shamikh, Alia, Basmaci, Elisa, Díaz De Ståhl, Teresita, Rajakumar, Timothy, Doultsinos, Dimitrios, Thrane, Kim, Ji, Andrew L., Khavari, Paul A., Tarish, Firaz, Tanoglidi, Anna, Maaskola, Jonas, Colling, Richard, Mirtti, Tuomas, Hamdy, Freddie C., Woodcock, Dan J., Helleday, Thomas, Mills, Ian G., Lamb, Alastair D., Lundeberg, Joakim
Published in Nature (London) (11.08.2022)
Published in Nature (London) (11.08.2022)
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Journal Article
Distal 22q11.2 microduplication encompassing the BCR gene
Descartes, Maria, Franklin, Judy, de Ståhl, Teresita Diaz, Piotrowski, Arkadiusz, Bruder, Carl E.G., Dumanski, Jan P., Carroll, Andrew J., Mikhail, Fady M.
Published in American journal of medical genetics. Part A (01.12.2008)
Published in American journal of medical genetics. Part A (01.12.2008)
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Journal Article
A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene
Mikhail, Fady M., Descartes, Maria, Piotrowski, Arkadiusz, Andersson, Robin, Diaz de Ståhl, Teresita, Komorowski, Jan, Bruder, Carl E.G., Dumanski, Jan P., Carroll, Andrew J.
Published in American journal of medical genetics. Part A (15.09.2007)
Published in American journal of medical genetics. Part A (15.09.2007)
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Journal Article
Genome-wide high-resolution analysis of DNA copy number alterations in NF1-associated malignant peripheral nerve sheath tumors using 32K BAC array
Mantripragada, Kiran K., de Ståhl, Teresita Díaz, Patridge, Chris, Menzel, Uwe, Andersson, Robin, Chuzhanova, Nadia, Kluwe, Lan, Guha, Abhijit, Mautner, Victor, Dumanski, Jan P., Upadhyaya, Meena
Published in Genes chromosomes & cancer (01.10.2009)
Published in Genes chromosomes & cancer (01.10.2009)
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Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progression
POPŁAWSKI, Andrzej B, JANKOWSKI, Michat, KACZMARCZYK, Aneta, BENETKIEWICZ, Magdalena, ANDERSSON, Robin, SANDGREN, Johanna, ZEGARSKA, Barbara, BALA, Dariusz, SRUTEK, Ewa, ALLISON, David B, PIOTROWSKI, Arkadiusz, ZEGARSKI, Wojciech, ERICKSON, Stephen W, DUMANSKI, Jan P, DIAZ DE STAHL, Teresita, PARTRIDGE, E. Christopher, CRASTO, Chiquito, JINGYU GUO, GIBSON, John, MENZEL, Uwe, BRUDER, Carl Eg
Published in European journal of human genetics : EJHG (01.05.2010)
Published in European journal of human genetics : EJHG (01.05.2010)
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Focal amplifications are associated with high grade and recurrences in stage Ta bladder carcinoma
Nord, Helena, Segersten, Ulrika, Sandgren, Johanna, Wester, Kenneth, Busch, Christer, Menzel, Uwe, Komorowski, Jan, Dumanski, Jan P., Malmström, Per‐Uno, de Ståhl, Teresita Díaz
Published in International journal of cancer (15.03.2010)
Published in International journal of cancer (15.03.2010)
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Journal Article
Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency
Díaz de Ståhl, Teresita, Grillner, Pernilla, Asmundsson, Jurate, Marino, Ana Maria, Holm, Stefan, Sandgren, Johanna, Nistér, Monica
Published in BioMed research international (01.01.2015)
Published in BioMed research international (01.01.2015)
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Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array
Nord, Helena, Hartmann, Christian, Andersson, Robin, Menzel, Uwe, Pfeifer, Susan, Piotrowski, Arkadiusz, Bogdan, Adam, Kloc, Wojciech, Sandgren, Johanna, Olofsson, Tommie, Hesselager, Göran, Blomquist, Erik, Komorowski, Jan, von Deimling, Andreas, Bruder, Carl E G, Dumanski, Jan P, Díaz de Ståhl, Teresita
Published in Neuro-oncology (Charlottesville, Va.) (01.12.2009)
Published in Neuro-oncology (Charlottesville, Va.) (01.12.2009)
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Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis
Sandgren, Johanna, Diaz de Ståhl, Teresita, Andersson, Robin, Menzel, Uwe, Piotrowski, Arkadiusz, Nord, Helena, Bäckdahl, Martin, Kiss, Nimrod B, Brauckhoff, Michael, Komorowski, Jan, Dralle, Henning, Hessman, Ola, Larsson, Catharina, Åkerström, Göran, Bruder, Carl, Dumanski, Jan P, Westin, Gunnar
Published in Endocrine-related cancer (01.09.2010)
Published in Endocrine-related cancer (01.09.2010)
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A segmental maximum a posteriori approach to genome-wide copy number profiling
Andersson, Robin, Bruder, Carl E. G., Piotrowski, Arkadiusz, Menzel, Uwe, Nord, Helena, Sandgren, Johanna, Hvidsten, Torgeir R., Diaz de Ståhl, Teresita, Dumanski, Jan P., Komorowski, Jan
Published in Bioinformatics (15.03.2008)
Published in Bioinformatics (15.03.2008)
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Journal Article
Occurrence of cancer in Marfan syndrome: Report of two patients with neuroblastoma and review of the literature
Maya‐González, Carolina, Delgado‐Vega, Angelica Maria, Taylan, Fulya, Lagerstedt Robinson, Kristina, Hansson, Lina, Pal, Niklas, Fagman, Henrik, Puls, Florian, Wessman, Sandra, Stenman, Jakob, Georgantzi, Kleopatra, Fransson, Susanne, Díaz De Ståhl, Teresita, Ek, Torben, Palmer, Ruth, Tesi, Bianca, Kogner, Per, Martinsson, Tommy, Nordgren, Ann
Published in American journal of medical genetics. Part A (01.12.2024)
Published in American journal of medical genetics. Part A (01.12.2024)
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